K-number	K130573
Device name	TYBER MEDICAL INTERBODY SYSTEM; ACIF, ALIF, PLIF, TLIF, DLIF
Applicant	Tyber Medical, LLC
Product code	ODP
Device class	Class II
Decision date	Sep 30, 2013
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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TYBER MEDICAL INTERBODY SYSTEM; ACIF, ALIF, PLIF, TLIF, DLIF

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